Canonical Allele Identifier: CA1953439071
Gene: FAR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728580C= , CM000673.2:g.13728580C= GRCh38
NC_000011.9:g.13750127C= , CM000673.1:g.13750127C= GRCh37
NC_000011.8:g.13706703C= NCBI36
NG_041826.1:g.64922C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*211-32C= ENSP00000515269.1:n.*211-32C=
ENST00000354817.8:c.1386-32C= MANE Select ENSP00000346874.3:n.1386-32C=
ENST00000354817.7:c.1386-32C= ENSP00000346874.3:n.1386-32C=
ENST00000532502.1:c.258-32C= ENSP00000434624.1:n.258-32C=
NM_032228.5:c.1386-32C= NP_115604.1:n.1386-32C=
XM_011520400.1:c.1395-32C= XP_011518702.1:n.1395-32C=
XM_011520401.1:c.1218-32C= XP_011518703.1:n.1218-32C=
XM_011520400.2:c.1395-32C= XP_011518702.1:n.1395-32C=
NM_032228.6:c.1386-32C= MANE Select NP_115604.1:n.1386-32C=